| Literature DB >> 30826368 |
Xi Chen1, Ping-Sheng Xu2, Zhen-Xing Zou3, Yang Liu2, Wen-Hao Zhou3, Qin Ren2, Dan Li2, Xiao-Min Li2, Kang-Ping Xu3, Gui-Shan Tan4.
Abstract
Six new neolignans, sinensiols B-G (1-6), together with three known analogues (7-9) were isolated from the whole plant of Selaginella sinensis. Their planar structures were established by comprehensive spectroscopic analyses including 1D, 2D NMR, IR and HRESIMS data. The absolute configurations of new compounds were elucidated by comparing their experimental CD spectra with known ones and using the reversed helicity rule for the 1Lb band ECD of dihydrobenzofuran neolignans. Sinensiols A-D (7, 1-3) belong to sesquilignan with a dimer of dihydrobenzo[b]furan moiety. The potential precursors of sinensiols A, B, D were also reported in this paper. In addition, all new compounds were screened for their cytotoxicity against A549 and HepG2 human cancer cell lines, and they didn't show inhibition on the growth of cancer cells.Entities:
Keywords: 2,3-dihydrobenzo[b]furan neolignans; Cytotoxicity; Selaginella sinensis; Sesquilignans
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Year: 2019 PMID: 30826368 DOI: 10.1016/j.fitote.2019.02.034
Source DB: PubMed Journal: Fitoterapia ISSN: 0367-326X Impact factor: 2.882